Syngene Associate Scientist Vacancy – M Pharma Apply

Syngene Associate Scientist Vacancy – M Pharma Apply

Syngene International Ltd. is an innovation-focused global discovery, development and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods and speciality chemical industries around the world. Syngene’ s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA and Herbalife. Its innovative culture is driven by the passion of its 4240- strong team of scientists who work with clients from around the world to solve their scientific problems, improve R&D productivity, speed up time to market and lower the cost of innovation.

Job Title: Associate Scientist

Job Location: Bangalore

Department: Discovery Biology

Educational Qualification:

M.Pharmacy

Technical/Functional Skills:

Understanding of DMPK related activity and instruments like Mass spectroscopy, HPLC, added advantages with the experience on Automation.
Expertise in preparation of DMPK related SOPs (study as well as instruments).

Experience:

Relevant experience of 3-6 years post qualification is required.

Behavioral Skills:

• Good work ethics.
• Good interpersonal skills, and the ability to work effectively in a team environment.
• Ability to work with co‐workers professionally.
• General ability to thrive in a growing infrastructure and culture and also think out of box approach when troubleshooting.

Job Purpose

The

incumbent will be responsible to support the Drug Metabolism and Pharmacokinetics (DMPK) group on the Quality and compliance-related activities.

Key Responsibilities:

• Review, document, and report all raw data, experimental procedures, documents and results according to GxP.
• Conduct QC review of departmental logbooks, equipment and instrument logs, equipment and software installation and validation documents, solution-reagent labels, reference standards, and controlled substances inventories.
• Support Regulatory Authority Inspections and Sponsor Audits.
  Assist team to ensure compliance to SOPs, suggest SOP revisions when applicable, and ensure reported and/or identified deviations to SOPs are properly documented in Study Report.
• Maintain the proper level of regulatory compliance for each study, helping to address QA audit findings.
• Maintain tools, computer programs, and SOPs required for studies.

Apply Online

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